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NCT03178916 Clinical Trial

Breast Feeding Practice in High Risk Pregnant Women

Breast Feeding Clinical Trial

Official title:
Breast Feeding Practice in High Risk Pregnant Women

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03178916
Other study ID # BFHRP
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2017
Est. completion date December 31, 2020

Study information
Verified date April 2021
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The American Academy of Paediatrics recognizes multiple benefits of breastfeeding to both the term and premature newborn, particularly with regard to protection from infectious agents. Studies have demonstrated decreased rates of bacteraemia, meningitis, respiratory and urinary tract infections, necrotizing enterocolitis, and otitis media among breastfed infants

Recruitment information / eligibility
Status Completed
Enrollment 140
Est. completion date December 31, 2020
Est. primary completion date October 31, 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria: 1. Diabetes mellitus. 2. Cardiac disease. 3. Essential hypertension. 4. Chronic chest disease, and/or chronic TB infection. 5. Chronic hepatitis. 6. Neurologic disease. 7. Anaemia (Hemoglobin <10 gm/dL). 8. Thyroid disease. 9. Multiple pregnancy. Exclusion Criteria: - pregnant women < 34 weeks.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Egypt Assiut Faculty of Medicine Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary The number of breast feeding women during pregnancy 6 months
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